AU2013351062A1

AU2013351062A1 - Tumor specific T-cell receptors

Info

Publication number: AU2013351062A1
Application number: AU2013351062A
Authority: AU
Inventors: Thomas Blankenstein; Gerald WILLIMSKY
Original assignee: Max Delbrueck Centrum fuer Molekulare in der Helmholtz Gemeinschaft
Current assignee: Max Delbrueck Centrum fuer Molekulare in der Helmholtz Gemeinschaft
Priority date: 2012-11-30
Filing date: 2013-11-29
Publication date: 2015-06-04
Anticipated expiration: 2033-11-29
Also published as: CN104853765B; EP2925349A1; AU2018203663A1; AU2020200092A1; CA2891967A1; WO2014083173A1; HK1214942A1; EP2925349B1; GB2508414A; AU2013351062B2; JP6615612B2; JP2015536665A; CN104853765A; US20150307585A1; US10683336B2

Abstract

The present invention relates to a method for the production of novel T-cell receptors (TCR) which provide a reduced risk of adverse events in immune therapy, specifically in adoptive T cell transfer. The TCRs produced according to the method of the invention are specific for tumor cells and do not react with healthy tissue. Furthermore provided are nucleic acids encoding the TCR of the invention, vectors and host cells comprising the TCRs of the invention as well as their use is the treatment of tumorous diseases.

Description

WO 2014/083173 PCT/EP2013/075141 TUMOR SPECIFIC T-CELL RECEPTORS FIELD OF THE INVENTION The present invention pertains to a method for the production of novel T-cell receptors (TCR) which provide a reduced risk of adverse events in immune therapy, specifically in adoptive T cell transfer. The TCRs produced according to the method of the invention are specific for tumor cells and do not react with healthy tissue. Furthermore provided are nucleic acids en coding the TCR of the invention, vectors and host cells comprising the TCRs of the invention as well as the use of these compounds in the treatment of tumorous diseases. DESCRIPTION Despite remarkable technological advancements in the diagnosis and treatment options avail able to patients diagnosed with cancer, the prognosis still often remains poor and many pa tients cannot be cured. Immunotherapy holds the promise of offering a potent, yet targeted, treatment to patients diagnosed with various tumors, with the potential to eradicate the malig nant tumor cells without damaging normal tissues. In theory the T cells of the immune system are capable of recognizing protein patterns specific for tumor cells and to mediate their de struction through a variety of effector mechanisms. Adoptive T-cell therapy is an attempt to harness and amplify the tumor-eradicating capacity of a patient's own T cells and then return these effectors to the patient in such a state that they effectively eliminate residual tumor, however without damaging healthy tissue. Although this approach is not new to the field of tumor immunology, still many drawbacks in the clinical use of adoptive T cell therapy impair the full use of this approach in cancer treatments. A TCR is a heterodimeric cell surface protein of the immunoglobulin super-family which is associated with invariant proteins of the CD3 complex involved in mediating signal transduc tion. TCRs exist in ap and y6 forms, which are structurally similar but have quite distinct ana tomical locations and probably functions. The extracellular portion of native heterodimeric ajTCR consists of two polypeptides, each of which has a membrane-proximal constant do main, and a membrane-distal variable domain. Each of the constant and variable domains in cludes an intra-chain disulfide bond. The variable domains contain the highly polymorphic WO 2014/083173 - 2 - PCT/EP2013/075141 loops analogous to the complementarity determining regions (CDRs) of antibodies. The use of TCR gene therapy overcomes a number of current hurdles. It allows equipping patients' own T cells with desired specificities and generation of sufficient numbers of T cells in a short period of time, avoiding their exhaustion. The TCR will be transduced into central memory T cells or T cells with stem cell characteristics, which may ensure better persistence and function upon transfer. TCR-engineered T cells will be infused into cancer patients ren dered lymphopenic by chemotherapy or irradiation, allowing efficient engraftment but inhibit ing immune suppression. Transgenic mice expressing human MHC molecules and a diverse human TCR repertoire serve as a tool to rapidly analyze whether peptide antigens are immu nogenic, i.e. are they efficiently processed and presented by MHC molecules, do they effi ciently induce T cell responses following immunization (Li et al. 2010 Nat Med). Using the human TCR transgenic mouse, any human peptide sequence not encoded by the mouse genome is suitable for immunization and will yield TCRs with optimal affinity. Opti mal affinity means that the T cells are restricted to human self-MHC molecules and recognize the peptide antigen as foreign, e.g. represent the non-tolerant repertoire. By using pep tide/MHC multimers, specific T cells of the transgenic mice can be sorted, human TCRs iso lated, e.g. by single cell PCR, the TCRs optimized for efficient expression while avoiding mispairing with endogenous TCR and used for transduction of patients' T cells with viral vec tors (Uckert et al. 2008 Cancer Immunol Immunother; Kammertoens T et al. 2009 Eur J Im munol). The key problem of ATT is to target the right antigen to prevent tumor recurrence and toxic side effects. This sounds simple given the large number of putative tumor antigens. However, most are tumor-associated (self) antigens (TAAs). TAAs are also expressed by normal cells. Expression by rare but vital cells has usually not been analyzed. Moreover, TAA expression may be heterogeneous within the tumor/metastases of a given individual. Thus, targeting TAAs bears the risk of ineffective long-term responses and destruction of normal tissues. Clinical trials with TCR (or chimeric antibody receptor; CAR)-engineered T cells, e.g. di rected against Melan-A/MART-1, gp 100, HER-2 and carcinoembryonic antigen, support this assumption.

WO 2014/083173 - - PCT/EP2013/075141 Morgan RA and colleagues present a case report on a patient with ERBB2 overexpressing cancer that was treated by infusing T cells transduced with a chimeric antigen receptor recog nizing ERBB2 into the patient. After 15 minutes of the infusion the patient experienced res piratory distress and dramatic pulmonary infiltrate. The patient died after 5 days. This dra matic outcome underlines the problem of toxic adverse effects in the context of adoptive T cell therapy. Another approach makes use of the immunization of mice, the subsequent isolation of the T cells and T cell receptors from these cells, in order to transduce autologous peripheral lym phocytes of a tumor patient. The transduced lymphocytes were expanded and then re-infused. Although tumor regression was observed, the patients still showed the destruction of normal cells (Johnson LA et al. 2009 Blood). Parkhurst and colleagues (2010 Mol Ther) genetically engineered autologous T lymphocytes of patients suffering from metastatic colorectal cancer refractory to standard treatments. The T lymphocytes were altered to express a murine T cell receptor directed at the carcinoembryonic antigen (CEA). Again the report shows regression of the tumor, however with severe transient inflammatory colitis as side effect in all patients. Thus, for many, if not most, tumor associated antigens substantial toxicity by effective adop tive T cell therapy is predictable. In view of the above described major drawbacks in the background art, it is the objective of the present invention to provide novel approaches for adoptive T-cell therapy which can over come the severe side effects observed in immune therapy when genetically engineered T cell receptors are introduced into autologous lymphocytes and re-infused into a human patient. A more specified object of the present invention is to provide novel antigen recognizing con structs which specifically target tumor cells and not healthy cells. In a first aspect of the present invention, the above objective is solved by a method for the production of a human T cell receptor (TCR) or a T-cell, which is specific for tumorous cells and has reduced adverse effects in adoptive T-cell therapy, comprising the method steps of a. Providing a host organism expressing un-rearranged human TCR loci, WO 2014/083173 PCT/EP2013/075141 b. Immunizing said host organism with a peptide comprising an epitope specific for a tumor specific antigen (TSA), c. Isolating from said host organism or cell a T cell clone having an activity against said human mutated TSA, d. Optionally, isolating from said T cell clone the TCR, wherein said TSA is selected out of the class of somatic mutated antigens. The surprising finding of the present invention is that if, by contrast to the state of the art ap proaches, mutant cancer-driving oncogenes, specifically TSAs out of the class of somatic mu tated antigens, are targeted by adoptive T cell therapy (ATT), many of the problems with TAAs as known in the state of the art are resolved. Except for antigens encoded by cancer viruses, mutated antigens are the only exclusively tumor-specific antigens. Of course, the TCRs produced in accordance with the herein described method of the inven tion do not only provide their advantageous effects in adoptive T cell therapy, but also in any other therapeutic approach wherein the specific binding of the TCR to its target is employed. The TCRs isolated in accordance with the method of the present invention are advantageous over the state of the art antigen recognizing constructs due to their reduced risk for adverse effects which are observed in adoptive T cell therapy. Adverse effects in context of adoptive T cell transfers are mainly due to autoimmune reactions or to off-target reactions. The present invention specifically intends to solve the former problem by providing T cells which are highly specific to tumor cells and do not mediate an immune reaction against a patient's healthy tissue. Adverse events following infusion of human autologous or allogeneic lym phocytes that the present invention seeks to reduce can be various. In a preferred embodiment of the present invention the TCR obtained by the present invention provide a reduced risk when used in adoptive T cell therapy for inducing healthy tissue damage, which might result in edema and necrosis. In one preferred embodiment of the present invention said host organism further comprises a transgene for the expression of a human major histocompatibility complex (MHC) class I or II allele. Preferably the MHC is a human leucocyte antigen (HLA) type which is known or sus pected to be able to present said mutated TSA. Even more preferred is that the HLA type which is expressed in said host organism is known or suspected to be able to present a peptide WO 2014/083173 PCT/EP2013/075141 derived from said mutated TSA. This peptide should comprise an amino acid sequence in cluding the mutation which is specifically present in the mutated TSA opposed to the corre sponding un-mutated (wild type) version of the same protein. HLAs corresponding to MHC class I comprise the types A, B, and C. HLA class I complexes present peptides which are processed inside the presenting cell (including alien peptides'such as viral peptides if present). In general, such HLA class I peptides are small polymers, about 9 amino acids in length. HLAs corresponding to MHC class II comprise the types DP, DM, DOA, DOB, DQ, and DR. HLA class II complexes present antigens originating from the out side of the cell. They can be of a length between 12 and 18 amino acids. The characterization of the responsible HLA alleles presenting an antigen of choice is a methodology generally known in the art. In said host organism used in accordance with the present invention - insofar it is not a hu man - the un-rearranged human TCR loci are preferably present as one or more transgenes in the genome of said host organism. Preferably these loci encode TCR a and 0 chains, and pref erably comprise a plurality, ideally all, of human TCR V, D, J, and/or C genes. For the method in accordance with the present invention it is preferably a prerequisite that said host organism has an adaptive immune system and/or is able to mount a VDJC rear rangement within said human TCR loci. Furthermore a host organism is preferred which is able to express heterologous TCRs. In certain preferred embodiments of the invention said host organism is a transgenic animal, preferably a mammal, more preferably a non-human mammal, most preferably a mouse, a rat, a donkey, a rabbit, a hare or a monkey, or any ani mal which is known in the art to be a host for the generation of T-cells. In the context of such embodiments of the invention which relate to the above method and wherein non-human host organisms are used, such a non-human host organism preferably further comprises inactivated endogenous TCR loci, preferably wherein said endogenous TCR loci encode for the TCR a and 0 chains of said non-human host organism. In one very specific embodiment of the present invention said host-organism is an "ABabDII" mouse. The term "ABabDII" mouse refers to the transgenic animal produced as described in Li et al., 2010;16:1029-34 Nature Medicine. Of course it is understood that also any other WO 2014/083173 - 6 - PCT/EP2013/075141 transgenic animal produced with the same methodology as described in Li et al. shall be en compassed as a suitable host organism for use in the herein described embodiments of the invention. An alternative embodiment relates to a method, wherein a human, for example a healthy indi vidual or a human patient suffering from a tumorous disease, is immunized with said peptide as described herein. In this embodiment T cells can be isolated subsequent to the immuniza tion process from the blood of the human subject. This embodiment has the advantage that the improved T cell receptor is expressed on human, ideally autologous, T cells which can then be used for reinfusion in adoptive T cell therapy. The peptide used for the immunization of the host organism in context of the method of the present invention comprises an amino acid sequence which is in at least one amino acid resi due mutated compared to the amino acid sequence of the corresponding wild-type cellular protein. The present invention relates to the use of tumor specific antigens, therefore proteins which were mutated in the development of tumor cells and thus in this specific mutated form exclusively are present in tumor cells. Normal, healthy, cells however might still express the original un-mutated (wild type) protein. Thus, for the herein described invention it is specifi cally preferred that the peptide used for immunization comprises in its sequence the mutation which differentiates the TSA from the original un-mutated cellular protein. Preferred peptides for use in the method of the invention comprise any of the sequences shown in SEQ ID No. 1 to 27. In preferred embodiments of the invention the peptide for immunization comprises the amino acid sequence shown in SEQ ID No. 1. Antigens which are specifically expressed in tumor cells and not in healthy tissue can be cate gorized into four types: (I) mutated antigens develop during tumor-genesis by point mutations or translocations within the tumor cells. Those antigens are strictly tumor-specific. In the con text of the invention these antigens are referred to as tumor specific antigens (TSA). (II) can cer/germline antigens are usually expressed solely within the germ cells of an adult organism and not in healthy somatic tissue. In cancer cells, however, due to the loss of epigenetic regu lation, germ-cell specific genes can be activated. (III) differentiation antigens are expressed in tumors and their healthy progenitor cells. CTL responses against such antigens often result in auto-immune reactions. (IV) overexpressed TAA show only minor expression in healthy cells WO 2014/083173 PCT/EP2013/075141 whereas in a tumor those antigens are strongly activated. For the present invention it is pre ferred that only antigens of the first type are used. For the invention TSAs formed by any kind of mutation are comprised. For merely illustrative reasons the following types of mutations are described: amino acid substitution, deletion, ad dition, insertion, or chemical or post-translational modification. Furthermore included are chromosomal translocations and exclusively in tumor cells expressed splice variants, for ex ample which occur by unspecific splicing mutations resulting in new splice sites. For the immunization process said peptide can have any length. A minimum requirement is however the presence of the epitope containing the above mentioned mutated sequence. Pre ferred peptides of the invention have a length of 100 amino acids, preferably of 50 amino ac ids, more preferably of 30 amino acids, even more preferably 8 to 16 amino acids. The exact peptide length might vary depending on whether the TSA is MHC class I or MHC class II presented. In order to enhance immunization of the host organism, it is preferred that an adjuvant is used together with the peptide. An adjuvant is for example, without being limiting thereto, CpG and/or incomplete Freunds adjuvant. After the initial immunization with the peptide, said host organisms is treated preferably at least one or two, three or four more times with said peptide and/or the adjuvant of choice. Freund's adjuvant is a solution of (mineral) oil wherein the antigen for immunization is emulsified. Incomplete Freund's adjuvant, as preferably used in this invention, does not contain any mycobacterial components. During and after the immunization process said host-organism should develop T cells ex pressing rearranged T cell receptors specific against the TSA of the invention. Such T-cell clones are then in a preferred embodiment isolated from said host organism. For example the cells can be isolated from spleen cells, lymph node cells or blood. T cell clones are selected for example via the surface expression of CD4 or CD8, depending on whether the TSA epitope is MHC class I or II. Methods for the isolation of single T cell clones form host or ganisms are well known for the person of skill in the art. The present invention is not restrict ed to a specific methodology for isolating T cells. However, in one preferred embodiment of the invention, said T cells or said T cell clone is after isolation further tested for the expres sion of a TCR binding to the TSA used in the method of the invention. This is preferably done WO 2014/083173 PCT/EP2013/075141 by tetramer binding (staining) using TSA specific HLA tetramers. Optionally, the isolated T cell or T cell clone is also tested for its specificity to the TSA compared with the un-mutated version of the cellular protein. To this end, T cell reactivity against peptides comprising the mutation and against peptides comprising the wild-type version is compared. In a preferred embodiment such T cells or T cell clones are isolated in accordance with the method of the invention, which are highly selective for the TSA and not the un-mutated version of the cellu lar protein. Another embodiment of the invention relates to a method as described herein, where after isolation of the T cell or T cell clone, the TCR sequence is cloned. In this embodiment the method in step d. as described above, comprises the further method steps of (i) preparing cDNA from said T-cell clone, and (ii) amplifying said cDNA, and (iii) cloning the respective TCR a and 0 genes into a vector. Preferably a retroviral vector for the transduction of human peripheral blood lymphocytes is used as a vehicle for the TCR of the invention. Means and methods for such a cloning procedure are well known to the skilled person. In another preferred embodiment of the invention the TSA used is expressed in a tumor cell or tumor disease. As used herein, the term "tumor " or "tumor disease" means both benign and malignant tu mors or neoplasms and includes melanomas, lymphomas, leukemias, carcinomas and sarco mas. Illustrative examples of tumor tissues are cutaneous such as malignant melanomas and mycosis fungoides; hematologic tumors such as leukemias, for example, acute lymphoblastic, acute myelocytic, or chronic myelocytic leukemia; lymphomas such as Hodgkin's disease or malignant lymphoma; gynecologic tumors such as ovarian and uterine tumors; urologic tu mors such as those of the prostate, bladder, or testis; soft tissue sarcomas, osseus, or non osseous sarcomas, breast tumors; tumors of the pituitary, thyroid, and adrenal cortex; gastro intestinal tumors such as those of the esophagus, stomach, intestine, and colon; pancreatic and hepatic tumors; laryngeae papillomestasas and lung tumors. Preferred tumors in the context of the present invention are selected from melanoma, lung tumor, endometrial tumors, glioma, lymphoma, leukemia or prostate tumor. Exemplary TSAs which can be subject to the inventive method described herein - without being limiting for the invention -are described in Krauthammer et al. 2012 (Nature Genetics).

WO 2014/083173 PCT/EP2013/075141 A preferred selection of TSAs which are presented by HLA type A2 are RAC1, RAC2, RHOTI, MAP2K1, MAP2K2, Nos1, EGFR, SMCA4, STKI1, ARID1A, RBM1O, U2AF1, EP300, CHD4, FBXW7, H3F3A, KLHL6, SPOP, or MED12. Their respective mutated epitope sequences are provided in the examples section herein below. The object of the present invention is furthermore solved by a nucleic acid molecule encoding for a TCR obtained or obtainable by the method in accordance with the present invention. Furthermore provided in the present invention are nucleic acid molecules which encode for the respective a a or 0 chains of an TCR of the invention, or for a variable or constant domain of a TCR of the invention, or for a fragment of a TCR of the invention, preferably wherein such a fragment of the TCR still has the activity/ability for binding its TSA. In addition to that, the nucleic acid molecule optionally has further sequences which are necessary for pro tein expression of the nucleic acid sequence, specifically for an expression in a mammali an/human, most preferably an immune cell. The nucleic acid used can be contained in a vector suitable for allowing expression of the nucleic acid sequence corresponding to the TCR in a cell. Also provided is a vector or a cell comprising a nucleic acid molecule described herein above, specifically wherein the vector is for use in medicine. Also a cell comprising a vector accord ing to the invention is provided. In another aspect the invention provides the T-cell receptor (TCR), or a fragment thereof, as obtained or obtainable by the method of the present invention. In this context it is specifically preferred that the TCR of the invention is a TCR which shows reduced adverse effects in im mune therapy. The TCR of the invention preferably does not target healthy cells or tissue, which express the un-mutated (wild-type) version of the TSA used for the generation of the TCR. The TCR of the invention in preferred embodiments does not induce necrosis events, and does not mount when given to subject an immune response against healthy cells or tissue. preferred TCR of the invention is a TCR specific for the epitope shown in SEQ ID No. 1. Preferably a TCR in accordance to the invention may be a TCR as described herein below. Yet another embodiment of the invention pertains to a single chain TCR (scTCR, preferably an a -scTCR, which are derived from a sequence of a TCR of the present invention. Single- WO 2014/083173 - 10 - PCT/EP2013/075141 chain TCRs (scTCRs) are artificial constructs consisting of a single amino acid strand. An scTCR can comprise a polypeptide of a variable region of a first TCR chain (e.g., an [alpha] chain) and a polypeptide of an entire (full-length) second TCR chain (e.g., a [beta] chain), or vice versa. Furthermore, the scTCR can optionally comprise one or more linkers which join the two or more polypeptides together. The linker can be, for instance, a peptide which joins together two single chains, as described herein. Also provided is such a scTCR of the invention or other TCR derived molecule of the inven tion, which is fused to a human cytokine, such as IL-2, IL-7 or IL-15. TCRs of the present invention can also be provided as a multimeric complex, comprising at least two scTCR or TCR molecules, wherein said scTCR or TCR molecules are interconnected for example by an introduced biotin-streptavidin functionality. In another aspect of the present invention a host cell is provided, comprising a vector a nucle ic acid or a TCR molecule as described herein above. In preferred embodiments of the inven tion the host cell is a human cell, preferably a human T-lymphocyte, which is positive for the expression of CD4 or CD8. Such a host cell of the invention is preferably obtained by trans duction of a nucleic acid or vector in accordance with the present invention. Transduction methods for introducing nucleic acid molecules into T cells are well known in the art and in clude without being limiting thereto viral transduction vehicles. In an alternative aspect of the invention a T-cell is provided obtained or obtainable by a meth od for the production of a human T cell receptor (TCR), which is specific for tumorous cells and has reduced adverse effects in adoptive T-cell therapy as described herein above. Such a T cell is depending on the host organism used in the method of the invention for example a human or non-human T-cell, preferably a non-human T-cell expressing a human TCR. The provided compounds of the invention are in a further aspect for use in medicine, for ex ample for use in the treatment of a cancerous disease, specifically wherein the cancerous dis ease is characterized by the specific expression of said mutated TSA. Most preferably the compounds of the invention are used in a cancer treatment that involves an adoptive T-cell transfer.

WO 2014/083173 11 PCT/EP2013/075141 Yet another aspect of the invention relates to a method of treating a human subject, specifical ly human subject suffering from a tumor disease. The method of treatment comprises the ad ministration of any of the aforementioned compounds into a patient in need of such a treat ment. The administration of the compounds of the invention can for example involve the infu sion of T cells of the invention into said patient. Preferably such T cells are autologous T cells of the patient which were in vitro transduced with a nucleic acid or TCR of the present inven tion. Thus also provided is a pharmaceutical composition, comprising a TCR or TCR fragment according to the invention, or a nucleic acid, a vector, a host cell, or an isolated T cell accord ing to the invention. In a preferred embodiment the pharmaceutical composition is for im mune therapy. Examples of pharmaceutically acceptable carriers or diluents useful in the present invention include stabilizers such as SPGA, carbohydrates (e.g. sorbitol, mannitol, starch, sucrose, glu cose, dextran), proteins such as albumin or casein, protein containing agents such as bovine serum or skimmed milk and buffers (e.g. phosphate buffer). Tumor antigens that are preferably used in the methods of the present invention to obtain a TCR of the invention are listed in tables 1 and 2 below (the mutation is indicated as amino acid exchange within the epitope in brackets): Table 1: Gene Protein Epitope Rac1 Ras-related C3 botulinum toxin substrate 1 27-35 (P29S) TRRAP transformation/transcription domain-associated protein 715-723 (S722F) Rac2 Ras-related C3 botulinum toxin substrate 2 28-36 (P29L) 28-36 (P29Q) Nos1 Nitric oxide synthase 770-779 (S771L) ARID1A AT-rich interactive domain-containing protein 1A 1999-2007 (E2000V) 1021-1031 (W1022L) H3F3A Histone H3.3 28-36 (G34V) KLHL6 Kelch-like protein 6 48-56 (F49L) ID3 Inhibitor of DNA binding 3 50-58 (L54V) FLT3 Fms-related tyrosine kinase 3 835-843 (D835Y) 835-843 (D835V) FBXW7 F-box/WD repeat-containing protein 7 456-464 (F462S) 456-464 (A463T) Med12 Mediator of RNA polymerase II transcription subunit 12 724-732 (D727E) CDK12 Cyclin-dependent kinase 12 898-906 (Y901C) CDC42 Cell division cycle 42 7-14 (G12V) SMARCA4 SWI/SNF related, matrix associated, actin dependent regulator 1153-1161 WO 2014/083173 - 12 - PCT/EP2013/075141 of chromatin, subfamily a, member 4 (G1 159W) SMO Smoothened, frizzled family receptor 412-420 (L412F) SF3B1 Splicing factor 3b, subunit 1 693-701 (K700E) CHD4 Chromodomain-helicase-DNA-binding protein 4 907-916 (L912V) SPOP Speckle-type POZ protein 83-91 (Y87N) 83-91 (Y87C) MAP2K2 Dual specificity mitogen-activated protein kinase2 154-162 (S154F) Notch1 Notch1 1568-1576 (L1 574P) 1592-1600 (R1598P) FOXA1 Forkhead Box Al 221-229 (D226N) 2nd NT5C2 5'-Nucleotidase, Cytosolic II a) 233-241 b) 236-244 (R238L) 2"d Bcr-Abl Bcr-Abl 247-255 (E255K) RHOT1 Mitochondrial Rho GTPase 1 29-37 (P30L) MAP2K1 Dual specificity mitogen-activated protein kinasel 20-28 (E20K) EGFR Epidermal growth factor receptor 717-725 (G719A) 1125-1133 (H1129Y) STK1 1 Serine/threonine-protein kinas 219-228 (P221L) RBM10 RNA-binding protein 10 316-324 (1316F) U2AF1 Splicing factor U2AF 26 kDa subunit 28-36 (S34F) EP300 Histone acetyltransferase p300 1623-1631 (R1627W) CDK4 Cyclin-dependent kinase 4 23-32 (R24C) 23-32 (R24L) PPP6C Protein phosphatase 6, catalytic subunit 269-277 (S270L) TACC1 Transforming, acidic coiled-coil containing protein 1 792-801 (C794F) KRAS V-Ki-ras2 Kirsten rat sarcoma viral oncogene homolog 5-14 (G12V) TRAF7 TNF receptor-associated factor 7, E3 ubiquitin protein ligase 518-527 (N520S) 531-541 (G536S) HIST1H3B Histone cluster 1, H3b 26-35 (K27M) ALK Anaplastic lymphoma receptor tyrosine kinase 1272-1280 (R1275Q) ABL1 C-abl oncogene 1, non-receptor tyrosine kinase 251-260 (E255K) 247-255 (E255V) CBL CbI proto-oncogene, E3 ubiquitin protein ligase 398-406 (H398Y) NPM1 Nucleophosmin (nucleolar phosphoprotein B23, numatrin) 283-291 (c.863_864insTCTG Insertion) 283-291 (c.863_864insCATG Insertion) 283-291 (c.863_864insCATG Insertion) EZH2 Enhancer of zeste homolog 2 637-645 (Y641 F) GNAS GNAS complex locus 201-210 (R201C) PDGFRA Platelet-derived growth factor receptor, alpha polypeptide 841-849 (D842V) TSHR Thyroid stimulating hormone receptor 451-459 (M453T) KIT V-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homo- 636-644 (K642E) log STAT3 Signal transducer and activator of transcription 3 a) 654-662 b) 659-667 (D661Y) CTNNB1 Catenin (cadherin-associated protein), beta 1 30-39 (S33C) 30-39 (S33F) 30-39 (S33Y) STK 1 Serine/threonine kinase 11 219-228 (P221L) ERBB2 V-erb-b2 erythroblastic leukemia viral oncogene homolog 2 773-782 (G776V) SLIT2 Slit homolog 2 8-16 (M81) CDKN2A Cyclin-dependent kinase inhibitor 2A 113-121 (P114L) XPO1 Exportin 1 568-576 (E571K) WO 2014/083173 - 13 - PCT/EP2013/075141 The above described TCR of the invention pertain in preferred embodiments to the following TCR molecules: The present invention pertains to a TCR alpha chain, comprising a CDR3 region with the se quence shown in any one of SEQ ID NO: 28, 30, 32, 33, 36, 38 or 40. Preferred are TCR al pha chains comprising a variable domain having the sequence shown in any one of SEQ ID NO 42, 44, 46, 47, 50, 52, or 54. The present invention pertains to a TCR beta chain, comprising a CDR3 region with the se quence shown in any one of SEQ ID NO: 29, 31, 34, 35, 37, 39 or 41. Preferred are TCR beta chains comprising a variable domain having the sequence shown in any one of SEQ ID NO 43, 45, 48, 49, 51, 53, or 55. Preferred embodiments of the invention pertain to specific TCR isolated, or produced (ob tained) according to any one of the methods as described herein. Such TCRs of the invention are preferably TCRs specific for targeting a mutated antigen selected from table 1 or 2. The Rac-1 or TRRAP mutated antigen are preferred. More specifically such TCRs are preferred which have the capacity to specifically bind to the mutated Rac-1 epitope FSGEYIPTV, or the mutated TRAPP epitope KLVFGSVFL. Preferred TCR of the present invention are furthermore characterized by the presence of a CDR3 region comprising any one of the amino acid sequences shown in SEQ ID NO. 28 to 41. A Rac-1 TCR in accordance with the invention, with an alpha or beta chain, preferably comprises a CDR3 having a sequence shown in any one of SEQ ID NO: 28 to 39. A pre ferred TRRAP TCR in accordance with the present invention is characterized by the presence of a CDR3 amino acid sequence selected from the sequence shown in SEQ ID NO: 40 or 41. More preferred is an alpha/beta TCR having an alpha chain comprising the CDR3 sequence shown in SEQ ID NO: 28, and a beta chain comprising the CDR3 sequence shown in SEQ ID NO: 29; an alpha/beta TCR having an alpha chain comprising the CDR3 sequence shown in SEQ ID NO: 30, and a beta chain comprising the CDR3 sequence shown in SEQ ID NO: 31; an alpha/beta TCR having an alpha chain comprising the CDR3 sequence shown in SEQ ID WO 2014/083173 -14- PCT/EP2013/075141 NO: 32, and a beta chain comprising the CDR3 sequence shown in SEQ ID NO: 34; an al pha/beta TCR having an alpha chain comprising the CDR3 sequence shown in SEQ ID NO: 32, and a beta chain comprising the CDR3 sequence shown in SEQ ID NO: 35; an alpha/beta TCR having an alpha chain comprising the CDR3 sequence shown in SEQ ID NO: 33, and a beta chain comprising the CDR3 sequence shown in SEQ ID NO: 34; an alpha/beta TCR hav ing an alpha chain comprising the CDR3 sequence shown in SEQ ID NO: 33, and a beta chain comprising the CDR3 sequence shown in SEQ ID NO: 35; an alpha/beta TCR having an al pha chain comprising the CDR3 sequence shown in SEQ ID NO: 36, and a beta chain com prising the CDR3 sequence shown in SEQ ID NO: 37; an alpha/beta TCR having an alpha chain comprising the CDR3 sequence shown in SEQ ID NO: 38, and a beta chain comprising the CDR3 sequence shown in SEQ ID NO: 39; an alpha/beta TCR having an alpha chain comprising the CDR3 sequence shown in SEQ ID NO: 40, and a beta chain comprising the CDR3 sequence shown in SEQ ID NO: 41. The TCR chains comprised in a TCR of the invention may furthermore comprise at least one, preferably two, most preferably all three CDR regions as present in one of the variable re gions of any one of TCR 1 to 7. The sequences of said variable regions which contain all three CDR regions are shown in SEQ ID NO 42 to 55. In another preferred embodiment the TCR of the invention comprises at least one variable region of an alpha and/or beta chain selected from a variable region of an alpha or beta chain of any one of the TCR TI to T7 of the invention as depicted herein below in table 3. The TCR as isolated in context of the present invention comprise the following variable re gions (CDR3 regions are underlined): Rac-1 TCR: TRAV20*02-CAVQTSQGGSEKLVF-TRAJ57*01 MEKMLECAFIV LWLQLGWLSG EDQVTQSPEA LRLQEGESSS LNCSYTVSGL RGLFWYRQDP GKGPEFLFTL YSAGEEKEKE RLKATLTKKE SFLHITAPKP EDSATYLCAV QTSQGGSEKL VFGKGTKLTV NPYIQNPEPA (SEQ ID NO:42) TRBV4-1*01-CASSQDASGIYYEQYF-TRBD2*02-TRBJ2-7*01 WO 2014/083173 - 15- PCT/EP2013/075141 MGCRLLCCAV LCLLGAVPID TEVTQTPKHL VMGMTNKKSL KCEQHMGHRA MYWYKQKAKK PPELMFVYSY EKLSINESVP SRFSPECPNS SLLNLHLHAL QPEDSALYLC ASSQDASGIY YEQYFGPGTR LTVT (SEQ ID NO:43) TRAV13-1*01-CAASRGGAQKLVF-TRAJ54*01 MTSIRAVFIF LWLQLDLVNG ENVEQHPSTL SVQEGDSAVI KCTYSDSASN YFPWYKQELG KGPQLIIDIR SNVGEKKDQR IAVTLNKTAK HFSLHITETQ PEDSAVYFCA ASRGGAQKLV FGQGTRLTIN PN (SEQ ID NO:44) TRBV3-1*01-CASSQLAGGPLYNEQFF-TRBD2*02-TRBJ2-1*01 MGCRLLCCVV FCLLQAGPLD TAVSQTPKYL VTQMGNDKSI KCEQNLGHDT MYWYKQDSKK FLKIMFSYNN KELIINETVP NRFSPKSPDK AHLNLHINSL ELGDSAVYFC ASSQLAGGPL YNEQFFGPGTRLTVL (SEQ ID NO:45) TRAV5*01-CAESKRFSDGQKLLF-TRAJ16*01 MR QVARVIVFLT LSMSRGEDVE QSLFLSVREG DSSVINCTYT DSSSTYLYWY KQEPGAGLQL LTYIFSNMDM KQDQRLTVLL NKKDKHLSLR IADTQTGDSA IYFCAESKRF SDGQKLLFAR GTMLKVDLN (SEQ ID NO:46) TRAV12-2*02-CAAQSARQLTF-TRAJ22*01 M MKSLRVLLVI LWLQLSWVWS QQKEVEQNSG PLSVPEGAIA SLNCTYSDRG SQSFFWYRQY SGKSPELIM SIYSNGDKED GRFTAQLNKA SQYVSLLIRD SQPSDSATYL CAAQSARQLT FGSGTQLTVL PD (SEQ ID NO:47) TRBV20-1*01(/02)-CSARDLITDTQYF-TRBJ2-3*01 MLLLLL LLGPGSGLGA VVSQHPSWVI CKSGTSVKIE CRSLDFQATT MFWYRQFPKQ SLMLMATSNE GSKATYEQGV EKDKFLINHA SLTLSTLTVT SAHPEDSSFY ICSARDLITD TQYFGPGTRL TVL (SEQ ID NO:48) TRBV3-1*01-CASSPWQETQYF-TRBJ2-5*01 MGCRLL CCVVFCLLQA GPLDTAVSQT PKYLVTQMGN DKSIKCEQNL GHDTMYWYKQ DSKKFLKIMF SYNNKELIIN ETVPNRFSPK SPDKAHLNLH INSLELGDSA VYFCASSPWQ ETQYFGPGTR LLVL (SEQ ID NO:49) WO 2014/083173 - 16- PCT/EP2013/075141 TRAV13-1*01 CAASLGSGNTPLVF TRAJ29*01 M TSIRAVFIFL WLQLDLVNGE NVEQHPSTLS VQEGDSAVIK CTYSDSASNY FPWYKQELGK GPQLIIDIRS NVGEKKDQRI AVTLNKTAKH FSLHITETQP EDSAVYFCAA SLGSGNTPLV FGKGTRLSVI AN (SEQ ID NO:50) TRBV28*01 CASSLHSGRDTQYF TRBJ2-3*01 TRBD2*02 MGIRLLCR VAFCFLAVGL VDVKVTQSSR YLVKRTGEKV FLECVQDMDH ENMFWYRQDP GLGLRLIYFS YDVKMKEKGD IPEGYSVSRE KKERFSLILE SASTNQTSMY LCASSLHSGR DTQYFGPGTR LTVL (SEQ ID NO:51) TRAV13-2*01 CAENRGANSKLTF TRAJ56*01 F MMAGIRALF MYLWLQLDWV SRGESVGLHL PTLSVQEGDN SIINCAYSNS ASDYFIWYKQ ESGKGPQFII DIRSNMDKRQ GQRVTVLLNK TVKHLSLQIA ATQPGDSAVY FCAENRGANS KLTFGKGITL SVRPD (SEQ ID NO:52) TRBV12-3*01 CASSFTGGFYGYTF TRBJ1-2*01 TRBD1*01 MDSWTFCCVS LCILVAKHTD AGVIQSPRHE VTEMGQEVTL RCKPISGHNS LFWYRQTMMR GLELLIYFNN NVPIDDSGMP EDRFSAKMPN ASFSTLKIQP SEPRDSAVYF CASSFTGGFY GYTFGSGTRL TVV (SEQ ID NO:53) TRRAP TCR: TRAV17*01-CATDWYTGANSKLTF-TRAJ56*01 METLLGVSLV ILWLQLARVN SQQGEEDPQA LSIQEGENAT MNCSYKTSIN NLQWYRQNSG RGLVHLILIR SNEREKHSGR LRVTLDTSKK SSSLLITASR AADTASYFCA TDWYTGANSK LTFGKGITLS VRPD (SEQ ID NO:54) TRBV6-2*01-CASSYSGYEQYF-TRBD1*01-TRBJ2-7*01 MSLGLLCCAA FSLLWAGPVN AGVTQTPKFR VLKTGQSMTL LCAQDMNHEY MYWYRQDPGM GLRLIHYSVG EGTTAKGEVP WO 2014/083173 - 17- PCT/EP2013/075141 DGYNVSRLKK QNFLLGLESA APSQTSVYFC ASSYSGYEQY FGPGTRLTVT (SEQ ID NO:55) One further preferred embodiment of the invention provides a TCR alpha and/or beta chain, or a fragment thereof, comprising a sequence selected from the group of SEQ ID NO 42 to 55. Preferably the TCR of the invention is heterodimeric TCR comprising an alpha chain comprising a sequence according to SEQ ID NO 42, and a beta chain comprising a sequence according to SEQ ID NO 43, or comprising an alpha chain comprising a sequence according to SEQ ID NO 44, and a beta chain comprising a sequence according to SEQ ID NO 45, or comprising an alpha chain comprising a sequence according to SEQ ID NO 46, and a beta chain comprising a sequence according to SEQ ID NO 48, or comprising an alpha chain com prising a sequence according to SEQ ID NO 46, and a beta chain comprising a sequence ac cording to SEQ ID NO 49, or comprising an alpha chain comprising a sequence according to SEQ ID NO 47, and a beta chain comprising a sequence according to SEQ ID NO 48, or comprising an alpha chain comprising a sequence according to SEQ ID NO 47, and a beta chain comprising a sequence according to SEQ ID NO 49, or comprising an alpha chain com prising a sequence according to SEQ ID NO 50, and a beta chain comprising a sequence ac cording to SEQ ID NO 51, or comprising an alpha chain comprising a sequence according to SEQ ID NO 52, and a beta chain comprising a sequence according to SEQ ID NO 53, or comprising an alpha chain comprising a sequence according to SEQ ID NO 54, and a beta chain comprising a sequence according to SEQ ID NO 55. In even more preferred aspects of the invention the TCR of the invention is a TCR comprising at least one TCR alpha or beta chain selected from the TCR chains of any one of TCRs TI to T7 in table 3 below. Most preferred is that the TCR of the invention is an alpha/beta TCR selected from any one of TI to T7 as depicted in table 3 herein below. The aforementioned TCRs of the invention may in some embodiments contain altered amino acid sequences. Preferred is that TCR chains are encompassed by the present invention which are at least 70, 80, 90, 95, 96, 97, 98, or 99 % identical to a TCR sequence, or TCR alpha or beta chain sequence, a TCR variable region according to any one of SEQ ID NO: 42 to 55, or a CDR3 sequence as disclosed herein. Most preferably a TCR of the invention comprises an WO 2014/083173 -18- PCT/EP2013/075141 alpha and/or beta chain which is at least 90%, or 95%, or 99% identical to an alpha/beta chain of any one of TCRs TI to T7 as depicted in table 3. The above described TCR are preferably specific for the mutated antigens of Rac-1 or TRRAP as disclosed in table 1 or 2, in particular when presented on a cell, such as a tumor cell or antigen presenting cell. Furthermore comprised by the present invention are functional fragments of the TCR or TCR chains of the invention. The term "functional fragment of the TCR or TCR chain" shall refer to a fragment of the full length receptor molecule, character ized in that the fragment is derived from that molecule and has maintained the same capability to bind the mutated TAA. In a further aspect, as already disclosed above, the invention also pertains to the nucleic acids encoding for the TCR molecules of the invention as well as cells comprising these nucleic acids, or cells expressing said TCRs of the invention. The invention furthermore pertains to the use of the TCR proteins or nucleic acids, or cells, in the various methods or uses described herein before. Preferably aspects of the invention relate to the treatment of tumorous diseases with the meth ods and various materials of the invention. Preferred diseases are cancers which are character ized by the expression of any one of the mutated TAA as disclosed herein. Preferred is a dis ease that is characterized by the expression of the mutated epitope of Rac- 1 or TRRAP. Pre ferred diseases treated with a TCR of the invention that is specific for the Rac-1 mutated anti gen or the TRRAP mutated antigen are selected from cancerous proliferative diseases, e.g. lung cancer, breast cancer, cervical cancer, colon cancer, gastric cancer, kidney cancer, leu kemia, liver cancer, lymphoma, ovarian cancer, pancreatic cancer, prostate cancer, rectal can cer, sarcoma, skin cancer, testicular cancer, and uterine cancer. Particular preferred diseases for RacI specific TCRs are melanoma and non-small cell lung cancer. The present invention will now be further described in the following examples with reference to the accompanying figures and sequences, nevertheless, without being limited thereto. For the purposes of the present invention, all references as cited herein are incorporated by refer ence in their entireties. In the Figures and Sequences: WO 2014/083173 - 19- PCT/EP2013/075141 Figure 1: shows the specific CD8+ T cell response against HLA-A201 restricted mutated RAC1P29S epitope in ABabDII mice. SEQ ID No 1 to 27: show mutated epitope sequences of HLA type A2 restricted TSAs as depicted in Table 1. SEQ ID No 28 to 41: show the CDR3 domain sequences of the TCR of the invention. SEQ ID No 42 to 55: show the variable regions of the TCR 1 to 7 of the invention.

WO 2014/083173 - 20 - PCT/EP2013/075141 EXAMPLES Exemplary tumor specific antigen epitopes which are usable and preferred in the context of the present invention are provided in table 2. Gene Protein H LAA2.LEpitope MELANOMA RAC1: Ras-related C3 botulinum toxin substrate 1 FP/SGEYIPTV RAC2: Ras-related C3 botulinum toxin substrate 1 FP/LGEYIPTV RHOT1: Mitochondrial Rho GTPase 1 FP/LEEVPPRA MAP2K1: Dual specificity mitogen-activated protein kinasel E/KIKLCDFGV MAP2K2: Dual specificity mitogen-activated protein kinase2 E/KIKLCDFGV S/FLDQVLKEA Nos1: Nitric oxide synthase KS/LQAYAKTL LUNG TUMOR EGFR: Epidermal growth factor receptor VLG/ASGAFGT SMCA4: Transcription activator BRG1 LLSTRAG/WGL STK1 1: Serine/threonine-protein kinas FQP/LPEIANGL ARID1A: AT-rich interactive domain-containing protein 1A MW/LVDRYLAFT FENMSKHPGL RBM10: RNA-binding protein 10 I/FLGALAPYA U2AF1: Splicing factor U2AF 26 kDa subunit RHGDRCS/FRL ENDOMETRIAL TUMORS EP300: Histone acetyltransferase p300 LMDGR/WDAFL LMDGR/QDAFL CHD4 Chromodomain-helicase-DNA-binding protein 4 NLEEL/VFHLL FBXW7: F-box/WD repeat-containing protein 7 TLYGHTF/SAV TLYGHTFA/TV GLIOMA H3F3A: Histone H3.3 QLATKAARK/M KSAPSTGNGV CLL KLHL6: Kelch-like protein 6 KF/LDDAGLSL PROSTATE TUMOR SPOP: Speckle-type POZ protein YLSLY/NLLLV YLSLY/CLLLV FVQGKDWGFN FVQGKDWGF/L MED12: Mediator of RNA polymerase II transcription subunit VLYD/EQPRHV 12 *wildtype/mutated amino acid WO 2014/083173 - 21 - PCT/EP2013/075141 Example 1: RAC1 specific TCR against the FSGEYIPTV Epitope For the generation of T-cells bearing a RAC 1 TSA specific TCR, mice deficient in their en dogenous TCR loci and expressing the human TCR repertoire were used. The production and setup of the transgenic mice (ABabDII mice) are in detail described elsewhere (Li LP, Lam pert JC, Chen X, Leitao C, Popovic J, Muller W, et al. Transgenic mice with a diverse human T cell antigen receptor repertoire. Nat Med. 2010;16:1029-34.). ABabDII mice were immunized twice with mutated RAC1P29S epitope (see above). Seven days after the last immunization, pooled spleen and lymph node cells were stimulated in vitro with RACI mutant or wildtype peptides and analyzed for expression of CD3, CD8 and intra cellular IFN-y. Figure 1 shows CD8+ and IFN-y+ cells within the CD3+ cell population (per centages indicated by numbers). In parentheses, the percentage of CD8+ and IFN-y+ T cells within the CD8+ T cell population is given. Example 2: RAC 1 and TRRAP specific TCR of the Invention Table 3: The following TCR could be isolated: peptide/purifi TCR Antigen cation TCR sequence CDR3* TRAV20*02-CAVQTSQGGSEKLVF Ti Rac-1 FSGEYIPTV TRAJ57*01 28 TRBV4-1*01-CASSQDASGIYYEQYF IFNg-CAPTURE TRBD2*02-TRBJ2-7*01 29 TRAV13-1*01-CAASRGGAQKLVF T2 Rac-1 FSGEYIPTV TRAJ54*01 30 TRBV3-1*01-CASSQLAGGPLYNEQFF IFNg-CAPTURE TRBD2*02-TRBJ2-1*01 31 TRAV5*01-CAESKRFSDGQKLLF T3/T4 Rac-1 FSGEYIPTV TRAJ16*01 32 TRAV12-2*02-CAAQSARQLTF A2-TETRAMER TRAJ22*01 33 TRBV20-1*01 (/02)-CSARDLITDTQYF TRBJ2-3*01 34 TRBV3-1*01-CASSPWQETQYF-TRBJ2 5*01 35 TRAV13-1*01 CAASLGSGNTPLVF T5 Rac-1 FSGEYIPTV TRAJ29*01 36 TRBV28*01 CASSLHSGRDTQYF A2-TETRAMER TRBJ2-3*01 TRBD2*02 37 TRAV13-2*01 CAENRGANSKLTF T6 Rac-1 FSGEYIPTV TRAJ56*01 F 38 A2-TETRAMER TRBV12-3*01 CASSFTGGFYGYTF 39 WO 2014/083173 - 22 - PCT/EP2013/075141 TRBJ1-2*01 TRBD1*01 TRAV17*01-CATDWYTGANSKLTF T7 TRRAP KLVFGSVFL TRAJ56*01 40 TRBV6-2*01-CASSYSGYEQYF IFNg-CAPTURE TRBD1*01-TRBJ2-7*01 41 *Sequence identifier Table 3 provides the sequences of the alpha and beta chains of the isolated TCR of the inven tion (TI to T7). The sequences are presented by the known TCR allele sequence and the spe cific CDR3 amino acid sequence of the TCR of the invention. TCR allele nomenclature is derived from the TCR allele Database IMGT (http://www.imgt.org/vquest/refseqh.html#VQUEST) Lefranc, M.-P. and Lefranc, G. The T cell receptor FactsBook Academic Press, London, UK (398 pages), (2001). The variable regions of the TCR chains of the TCR 1 to 7 are provided in SEQ ID No 42 to 55. For T3/T4, the inventors discovered that in particular the chain combination TRAV5/TRBV20-1 (SEQ ID NO: 32 and34) shows good binding to the RacI-tetramer.

Claims

1. A method for the production of a human T cell receptor (TCR), which is specific for tumorous cells and has reduced adverse effects in adoptive T-cell therapy, comprising a. Providing a host organism expressing unrearranged human TCR loci, b. Immunizing said host organism with a peptide comprising an epitope specific for a tumor specific antigen (TSA), c. Isolating from said host organism a T cell clone having an activity against said human mutated TSA, d. Optionally, isolating from said T cell clone the TCR, wherein said TSA is selected out of the class of somatic mutated antigens.

2. The method according to claim 1, wherein said host organism further comprises a transgene for the expression of a human major histocompatibility complex (MHC) class I or II, preferably the human leucocyte antigen (HLA) type which is known to present said mutated TSA.

3. The method according to claim 1 or 2, wherein said unrearranged human TCR loci are present as one or more transgenes in the genome of said host organism.

4. The method according to any one of claims 1 to 3, wherein said human TCR loci en code TCR a and 0 chains, and preferably comprise a plurality of TCR V, D, J, and/or C genes.

5. The method according to any one of claims 1 to 4, wherein said host organism has an adaptive immune system and/or is able to mount a VDJC rearrangement and expres sion of heterologous TCRs; preferably said host organism is a transgenic animal, pref erably a mammal, more preferably a non-human mammal, most preferably a mouse, a rat, a donkey, a rabbit, a hare or a monkey. WO 2014/083173 PCT/EP2013/075141 - 24

6. The method according to any one of claims 1 to 3, wherein said host organism further comprises inactivated endogenous TCR loci, preferably wherein said endogenous TCR loci encode for TCR a and 0 chains.

7. The method according to any one of claims 1 to 4, wherein said host organism is an ABabDII mouse.

8. The method according to any one of claims 1 to 7, wherein said peptide comprises an amino acid sequence which is in at least one amino acid residue mutated compared to the amino acid sequence of the corresponding wild-type cellular protein.

9. The method according to claim 8, wherein a mutation is selected from a substitution, deletion, addition, insertion, chromosomal translocation or chemical or post translational modification of said at least one amino acid residue.

10. The method according to any one of claims I to 9, wherein said peptide has a length of 100 amino acids, preferably of 50 amino acids, more preferably of 30 amino acids, even more preferably 8 to 16 amino acids.

11. The method according to any one of claims I to 10, wherein in step b. CpG and in complete Freunds adjuvant is additionally administered to said host-organism to en hance immunization efficiency.

12. The method according to any one of claims I to 11, wherein after initial immunization, said host organisms is treated at least one or more times with said peptide plus CpG and incomplete Freunds adjuvant.

13. The method according to any one of claims 1 to 12, wherein said T-cell clone is isolat ed from spleen cells, lymph node cells or blood of said host organism.

14. The method according to any one of claims I to 13, wherein step d., comprises the fur ther method steps of (i) preparing cDNA from said T-cell clone, and (ii) amplifying said cDNA, and (iii) cloning the respective TCR a and 0 genes into a vector.

15. The method according to claim 14, wherein said vector is a retroviral vector for the transduction of human peripheral blood lymphocytes. WO 2014/083173 - 25 - PCT/EP2013/075141

16. The method according to any one of claims 1 to 15, wherein said mutated TSA is ex pressed in a tumor selected from melanoma, lung tumor, endometrial tumors, glioma, lymphoma, leukemia or prostate tumor.

17. The method according to any one of claims 1 to 15, wherein said mutated TAA is se lected from RACI, RAC2, RHOTI, MAP2K1, MAP2K2, Nos1, EGFR, SMCA4, STKI, ARID1A, RBM1O, U2AF1, EP300, CHD4, FBXW7, H3F3A, KLHL6, SPOP, or MED12.

18. A nucleic acid molecule encoding for a TCR obtained by the method according to any one of claims 1 to 17, or for an a or 0 chain thereof, or for a variable or constant do main thereof, or for a fragment thereof having the ability to bind to said mutated TSA.

19. A vector comprising a nucleic acid according to claims 18.

20. A TCR obtainable by a method according to any one of claims 1 to 17, or a a or chain thereof, or a variable or constant domain thereof, or a fragment thereof having the ability to bind to said mutated TAA antigenic fragments thereof.

21. A TCR comprising an alpha and/or beta chain, wherein said alpha and/or beta chain comprises at least one CDR3 domain according to any one of SEQ ID NO: 28 to 41.

22. The TCR according to claim 21, wherein said TCR comprises at least one variable re gion selected from a variable region of a TCR single chain of any one of TCR TI to T7 in table 3, preferably wherein said variable region comprises a sequence according to any one of SEQ ID NO 42 to 55.

23. A host cell, comprising a vector according to claim 19, a nucleic acid according to claim 18 or a TCR according to any one of claims 20 to 22.

24. The host cell according to claim 23, which is a human cell, preferably a T-cell.

25. The host cell according to claim 23, which is a CD4 or CD8 positive T-cell.

26. A non-human T-cell, obtainable by a method according to any one of claims I to 17.

27. The non-human T-cell according to claim 26, wherein the T-cell is a non-human T-cell expressing a human TCR. WO 2014/083173 PCT/EP2013/075141 - 26

28. A nucleic acid molecule according to claim 18, a vector according to claim 19, a TCR according to any one of claims 20 to 22 or a host cell according to any one of claims 23 to 25, for use in medicine.

29. The nucleic acid molecule, a vector, a TCR or a host cell according to claim 28, for use in the treatment of a cancerous disease, specifically wherein the cancerous disease is characterized by the specific expression of said mutated TSA.

30. The nucleic acid molecule, a vector, a TCR or a host cell according to claim 29, wherein said treatment involves adoptive T-cell therapy.